Palm Beach Gardens, Florida, United States
$90/hr · Starting at $25
Quality, Regulatory Affairs and Compliance Consultant for the medical device, life science, fields..
Miami, Florida, United States
$50/hr · Starting at $25
The services I can assist with include: PRE-MARKET RELATED POST-MARKET RELATED GENERAL REGULATORY AFFAIRS - Regulatory project management - Regulatory/Compliance strategy development - Workshops and
Hyderabad, Telangana, India
$15/hr · Starting at $30
Expertise in Pharma Regulatory intelligence which involves research on the latest regulatory updates
$10/hr · Starting at $25
1) expertise on regulatory fillings to USFDA and DCGI(CDSCO, SUGAM, NDPS, CBN). 2) expertise on ICH and Drugs and cosmetics acts and Narcotics act
Ben Aknoun, Alger, Algeria
$25/hr · Starting at $25
I am a regulatory affairs pharmacist with more than 8 years experience in regulatory affairs. Having a good knowledge of the local pharma environment, I can support and represent companies in Algeria
Bhavnagar, Gujarat, India
$8/hr · Starting at $25
Regulatory Affairs Services includes DMF, ASMF, CQA, ICH, USFDA, MCH and DCGI Documentation etc.Genuine and Transparent Service
Nairobi, Nairobi Area, Kenya
$120/hr · Starting at $110
Provide comprehensive Regulatory services across the spectrum of global product development, registration and commercialization. Specializes in Dossier strategy, Dossier Gap Analysis, Dossier Compilat…
Mysuru, Karnataka, India
$30/hr · Starting at $150
Glova Pharma Solution is a startup founded in 2018 by young professional to support pharmaceutical and life sciences companies to garner pharmaceutical regulatory licenses, regulatory strategy to garn…
Chandigarh, Chandigarh, India
$40/hr · Starting at $30
I had an extensive Pharmaceutical industrial experience in Regulatory Affairs Department as Manager. In addition I worked as Pharmaceutical lecturer and taught B.Pharm and M.Pharm students and took bo…
Jacksonville Beach, Florida, United States
Past Earnings
$125/hr · Starting at $35
Provides medical device manufacturers expert guidance in meeting global medical device regulatory compliance such as, US FDA and CE Marking. Experience in developing ISO 13485, FDA QSR, cGMP, CMDCAS,…
Pune, Maharashtra, India
$9/hr · Starting at $50
Provide End to end regulatory solutions as below: US/EU - Submissions in CTD/eCTD format with Due diligence and compilation Asian submissions Indian submission Other countries product registrations.
Eden Prairie, Minnesota, United States
$50/hr · Starting at $35
Provide strategic and tactical direction for all regulatory, clinical, product safety, design, registration and post-market surveillance activities. Provide regulatory assistance on medical devices, O…
Fort Wright, Kentucky, United States
$150/hr · Starting at $100
I provide complete support from preparing initial pre-IND packages and FDA meetings, to developing all modules of the IND for submission. I can support you as you develop your NDA or BLA to bring a dr…
Campinas, Sao Paulo, Brazil
$200/hr · Starting at $25
The regulatory process from product design to market entry for a new medical device or IVD is oftentimes complicated and unclear. In Brazil, it can also become difficult to make a clear distinction be…
Bengaluru, Karnataka, India
$5/hr · Starting at $25
Siddharth Gupta is a Chartered Accountant and a law graduate. He has over 10 years of experience in the tax and regulatory space. He has represented clients before the regulatory authorities at variou…
Chicago, Illinois, United States
$40/hr · Starting at $25
I am an independent regulatory consultant who works with manufacturers to ensure the compliance of company documents with the latest regulations at the state and federal level. To date, my experience
Vilnius, Vilnius, Lithuania
$25/hr · Starting at $50
Anton Sudnik can help you with all regulatory and compliance issues. Anton will ensure that your business is in compliance with all necessary regulations and standards. The Regulatory Compliance Advis…
Mumbai, Maharashtra, India
$10/hr · Starting at $90
I am into Regulatory Affairs since 3 years. Following are the services :- 1) Dossier preparation as per different country's guidelines. 2) CTD format dossier preparation 3) Dealing and resolving dif…
Kazhakkoottam, Kerala, India
$15/hr · Starting at $25
Experienced regulatory document publisher and medical writing quality reviewer. Tasks Familiar: Document publishing(All clinical documents) Quality check(All clinical documents) Data entry,PDF merging…
$10/hr · Starting at $30
Quality and Regulatory consultant for medical devices , support in creating DHF file , Preparation of Risk Management plan , Preparation of hazard analysis , FMEA ,Reviewing User manuals , Technical f…